Interesting facts
Interesting Facts about 3-(2-Hydroxyphenyl)propanoic Acid
3-(2-Hydroxyphenyl)propanoic acid, commonly known for its intriguing structure and potential applications, captivates the interest of chemists and students alike. Here are some fascinating aspects of this compound:
- Structural Composition: This compound is notable for having a hydroxyl group (-OH) attached to a phenyl ring, which influences its reactivity and solubility.
- Biological Relevance: Compounds similar to this have been studied for their antioxidant properties, offering potential benefits in pharmaceutical and nutraceutical applications.
- Natural Sources: It is often found in various plants, contributing to the complex chemistry of flavonoids and phenolic compounds, which are crucial in many natural biological processes.
- Applications: Researchers are exploring its potential in:
- Food industry as a preservative due to its ability to inhibit oxidation.
- Cosmetics for its protective effects against skin aging.
- Pharmaceutical formulations for improved drug delivery systems.
- Synthesis Approaches: The synthesis of 3-(2-hydroxyphenyl)propanoic acid involves various methods, often utilizing techniques like:
- Condensation reactions.
- Oxidative procedures from simpler starting materials.
In summary, 3-(2-hydroxyphenyl)propanoic acid stands out due to its potential in multiple fields ranging from health to industrial applications. As research continues, this compound may reveal even more exciting possibilities!
Synonyms
3-(2-hydroxyphenyl)propanoic acid
495-78-3
3-(2-Hydroxyphenyl)propionic acid
Melilotic acid
Benzenepropanoic acid, 2-hydroxy-
2-hydroxybenzenepropanoic acid
melilotate
o-Hydroxyphenylpropionic acid
3-(o-Hydroxyphenyl) propionic acid
hydrocoumaric acid
2-Hydroxyphenylpropanoate
UNII-CN1RK42MAD
CN1RK42MAD
2-hydroxyhydrocinnamic acid
O-Hydroxyhydrocinnamic acid
beta-(O-Hydroxyphenyl)propionic acid
MFCD00014026
2-HYDROXY-BENZENEPROPANOIC ACID
HYDRO-O-COUMARIC ACID
CHEBI:16104
HYDROCINNAMIC ACID, O-HYDROXY-
Propanoic acid, 3-(2-hydroxyphenyl)-
3-(2-Hydroxyphenyl) propionate
Melilotsaure
o-hydrocoumaric acid
bmse000331
Oprea1_380863
SCHEMBL35529
DTXSID2075421
3-(2-hydroxyphenyl)propanoicacid
3-(o-hydroxyphenyl)propionic acid
HMS1789F10
2-Hydroxybenzenepropanoic acid, 9CI
3-(2-Hydroxyphenyl) propanoic acid
3(2-HYDROXYPHENYL)PROPANOATE
s3339
STL565788
3-(2-hydroxy-phenyl)-propionic acid
beta -(O-hydroxyphenyl)propionic acid
AKOS000121351
.beta.-(O-Hydroxyphenyl)propionic acid
CS-W017874
FH54991
FS-1546
HY-W017158
MB00231
3-(O-Hydroxyphenyl)propionic acid, 8CI
3-(2-Hydroxyphenyl)propionic acid, 99%
SY101015
DB-021594
NS00074024
EN300-16621
C01198
F16128
Q11751633
Z56347225
4FD9685D-2A23-40E8-8F8B-013949003BDF
InChI=1/C9H10O3/c10-8-4-2-1-3-7(8)5-6-9(11)12/h1-4,10H,5-6H2,(H,11,12
Solubility of 3-(2-hydroxyphenyl)propanoic acid
The solubility characteristics of 3-(2-hydroxyphenyl)propanoic acid (C9H10O3) are intriguing due to the presence of both hydrophobic and hydrophilic functional groups in its molecular structure. This compound features a hydrophilic hydroxyl group as well as a carboxylic acid, which can engage in hydrogen bonding, enhancing its solubility in polar solvents.
Key aspects of its solubility include:
In summary, the solubility of 3-(2-hydroxyphenyl)propanoic acid can be described as moderate to good in polar environments, which makes it a compound of interest in various chemical and pharmaceutical applications. Its ability to engage in hydrogen bonding is a key factor contributing to its solubility profile.